HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353195Generated: October 30, 2026
Sodium Bicarbonate → tert-Butyl 2-methyl-2-[4-({[(4-methyl-1,3-oxazol-5-yl)methyl]amino}methyl)-phenoxy]-propanoate
https://huagongshe.com/reaction/353195
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | tert-Butyl 2-(4-formylphenoxy)-2-methylpropanoate | HCID 22708193 | — |
| Reactant | (4-Methyl-1,3-oxazol-5-yl)methylamine | HCID 22708194 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | tert-Butyl 2-methyl-2-[4-({[(4-methyl-1,3-oxazol-5-yl)methyl]amino}methyl)-phenoxy]-propanoate | HCID 22708253 | — |
Reaction Steps
1.25 g (4.73 mmol) of tert-butyl 2-(4-formylphenoxy)-2-methylpropanoate (Example I-4) and 0.64 g (5.67 mmol) of (4-methyl-1,3-oxazol-5-yl)methylamine (Example III-28) are together initially charged in 1,2-dichloroethane. At room temperature, 1.50 g (7.09 mmol) of sodium triacetoxyborohydride are added. The reaction mixture is stirred at room temperature for 4 hours and then admixed with saturated sodium bicarbonate solution and extracted with ethyl acetate. The organic phase is dried over magnesium sulphate and freed from the solvent under reduced pressure. The residue is purified chromatographically on silica gel (dichloromethane/methanol 30:1) and then dried under reduced pressure. This gives 1.104 g (65% of theory) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06750236B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-15aa678edc724d93a93c78d1067b1645 |
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| Source note | uspto-grants-2004_06 |
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